@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_head
{
this:
np:hasAssertion
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_assertion
;
np:hasProvenance
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_provenance
;
np:hasPublicationInfo
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_assertion
a
np:Assertion
.
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_provenance
a
np:Provenance
.
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_assertion
{
miriam-gene:1750
a
ncit:C16612
.
lld:C2931019
a
ncit:C7057
.
dgn-gda:DGN8978087c33bdbee802f7af7389cb92ad
sio:SIO_000628
miriam-gene:1750
,
lld:C2931019
;
a
sio:SIO_001121
.
}
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_provenance
{
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_assertion
dcterms:description
"[Both deletions included the known genes associated with SHFM1 (DLX5, DLX6 and DSS1), whereas in the third patient one of the inversion break points was located just centromeric to these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19401716
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP840138.RArvzaSwhl0Ru93DQR767sMqOJpPtpl1bqpnuGJ7_EuWw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:33+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}